Literature DB >> 18241076

X-linked congenital ataxia: a new locus maps to Xq25-q27.1.

Ginevra Zanni1, Enrico Bertini, Cecelia Bellcross, Brigitte Nedelec, Guy Froyen, Gerhard Neuhäuser, John M Opitz, Jamel Chelly.   

Abstract

We report clinical and molecular studies on a large American family of Norwegian descent with X-linked nonprogressive congenital ataxia (XCA) in six affected males over three generations. Neuroimaging showed global cerebellar hypoplasia without evidence of supratentorial anomalies. Linkage analysis resulted in a maximum LOD score Z = 3.44 for marker DXS1192 at Theta = 0.0 with flanking markers DXS1047 and DXS1227 defining a region of 12 cM in Xq25-q27.1. The clinical and neuroradiological findings in the present family are very similar to those described in two reported X-linked families [Illarioshkin et al., 1996; Bertini et al., 2000]; however, the newly identified locus does not overlap with the one defined previously, indicating that there are at least two genes responsible for this rare form of X-linked congenital cerebellar ataxia with normal intelligence. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18241076     DOI: 10.1002/ajmg.a.32186

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  7 in total

1.  Polarized localization of voltage-gated Na+ channels is regulated by concerted FGF13 and FGF14 action.

Authors:  Juan Lorenzo Pablo; Chaojian Wang; Matthew M Presby; Geoffrey S Pitt
Journal:  Proc Natl Acad Sci U S A       Date:  2016-04-04       Impact factor: 11.205

2.  A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasia.

Authors:  Eleonora Di Gregorio; Federico T Bianchi; Alfonso Schiavi; Alessandra M A Chiotto; Marco Rolando; Ludovica Verdun di Cantogno; Enrico Grosso; Simona Cavalieri; Alessandro Calcia; Daniela Lacerenza; Orsetta Zuffardi; Saverio Francesco Retta; Giovanni Stevanin; Cecilia Marelli; Alexandra Durr; Sylvie Forlani; Jamel Chelly; Francesca Montarolo; Filippo Tempia; Hilary E Beggs; Robin Reed; Stefania Squadrone; Maria C Abete; Alessandro Brussino; Natascia Ventura; Ferdinando Di Cunto; Alfredo Brusco
Journal:  J Med Genet       Date:  2013-06-07       Impact factor: 6.318

Review 3.  Fibroblast Growth Factor Homologous Factors: New Roles in Neuronal Health and Disease.

Authors:  Juan L Pablo; Geoffrey S Pitt
Journal:  Neuroscientist       Date:  2014-12-09       Impact factor: 7.519

Review 4.  X-linked disorders with cerebellar dysgenesis.

Authors:  Ginevra Zanni; Enrico S Bertini
Journal:  Orphanet J Rare Dis       Date:  2011-05-15       Impact factor: 4.123

5.  The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children.

Authors:  Alessandra Terracciano; Florence Renaldo; Ginevra Zanni; Adele D'Amico; Anna Pastore; Sabina Barresi; Enza Maria Valente; Fiorella Piemonte; Giulia Tozzi; Rosalba Carrozzo; Massimiliano Valeriani; Renata Boldrini; Eugenio Mercuri; Filippo Maria Santorelli; Enrico Bertini
Journal:  Eur J Paediatr Neurol       Date:  2011-08-27       Impact factor: 3.140

6.  Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxia.

Authors:  Karla P Figueroa; Sharan Paul; Tito Calì; Raffaele Lopreiato; Sukanya Karan; Martina Frizzarin; Darren Ames; Ginevra Zanni; Marisa Brini; Warunee Dansithong; Brett Milash; Daniel R Scoles; Ernesto Carafoli; Stefan M Pulst
Journal:  Dis Model Mech       Date:  2016-03-24       Impact factor: 5.758

7.  Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis.

Authors:  Ginevra Zanni; Tito Calì; Vera M Kalscheuer; Denis Ottolini; Sabina Barresi; Nicolas Lebrun; Luisa Montecchi-Palazzi; Hao Hu; Jamel Chelly; Enrico Bertini; Marisa Brini; Ernesto Carafoli
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-21       Impact factor: 11.205

  7 in total

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